BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

662 related articles for article (PubMed ID: 25849321)

  • 1. Genes with de novo mutations are shared by four neuropsychiatric disorders discovered from NPdenovo database.
    Li J; Cai T; Jiang Y; Chen H; He X; Chen C; Li X; Shao Q; Ran X; Li Z; Xia K; Liu C; Sun ZS; Wu J
    Mol Psychiatry; 2016 Feb; 21(2):290-7. PubMed ID: 25849321
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Cross-Disorder Analysis of De Novo Mutations in Neuropsychiatric Disorders.
    Li K; Fang Z; Zhao G; Li B; Chen C; Xia L; Wang L; Luo T; Wang X; Wang Z; Zhang Y; Jiang Y; Pan Q; Hu Z; Guo H; Tang B; Liu C; Sun Z; Xia K; Li J
    J Autism Dev Disord; 2022 Mar; 52(3):1299-1313. PubMed ID: 33970367
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Estimating contribution of rare non-coding variants to neuropsychiatric disorders.
    Takata A
    Psychiatry Clin Neurosci; 2019 Jan; 73(1):2-10. PubMed ID: 30293238
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identification of De Novo DNMT3A Mutations That Cause West Syndrome by Using Whole-Exome Sequencing.
    Liu Z; Li Z; Zhi X; Du Y; Lin Z; Wu J
    Mol Neurobiol; 2018 Mar; 55(3):2483-2493. PubMed ID: 28386848
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Implications of de novo mutations in guiding drug discovery: A study of four neuropsychiatric disorders.
    So HC; Wong YH
    J Psychiatr Res; 2019 Mar; 110():83-92. PubMed ID: 30597425
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Gene4Denovo: an integrated database and analytic platform for de novo mutations in humans.
    Zhao G; Li K; Li B; Wang Z; Fang Z; Wang X; Zhang Y; Luo T; Zhou Q; Wang L; Xie Y; Wang Y; Chen Q; Xia L; Tang Y; Tang B; Xia K; Li J
    Nucleic Acids Res; 2020 Jan; 48(D1):D913-D926. PubMed ID: 31642496
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism.
    Chen R; Davis LK; Guter S; Wei Q; Jacob S; Potter MH; Cox NJ; Cook EH; Sutcliffe JS; Li B
    Mol Autism; 2017; 8():14. PubMed ID: 28344757
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Varying Intolerance of Gene Pathways to Mutational Classes Explain Genetic Convergence across Neuropsychiatric Disorders.
    Shohat S; Ben-David E; Shifman S
    Cell Rep; 2017 Feb; 18(9):2217-2227. PubMed ID: 28249166
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Targeted sequencing and functional analysis reveal brain-size-related genes and their networks in autism spectrum disorders.
    Li J; Wang L; Guo H; Shi L; Zhang K; Tang M; Hu S; Dong S; Liu Y; Wang T; Yu P; He X; Hu Z; Zhao J; Liu C; Sun ZS; Xia K
    Mol Psychiatry; 2017 Sep; 22(9):1282-1290. PubMed ID: 28831199
    [TBL] [Abstract][Full Text] [Related]  

  • 10. mirTrios: an integrated pipeline for detection of de novo and rare inherited mutations from trios-based next-generation sequencing.
    Li J; Jiang Y; Wang T; Chen H; Xie Q; Shao Q; Ran X; Xia K; Sun ZS; Wu J
    J Med Genet; 2015 Apr; 52(4):275-81. PubMed ID: 25596308
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Truncating variant burden in high-functioning autism and pleiotropic effects of LRP1 across psychiatric phenotypes.
    Torrico B; Shaw AD; Mosca R; Vivó-Luque N; Hervás A; Fernàndez-Castillo N; Aloy P; Bayés M; Fullerton JM; Cormand B; Toma C
    J Psychiatry Neurosci; 2019 Sep; 44(5):350-359. PubMed ID: 31094488
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Whole exome sequencing coupled with unbiased functional analysis reveals new Hirschsprung disease genes.
    Gui H; Schriemer D; Cheng WW; Chauhan RK; Antiňolo G; Berrios C; Bleda M; Brooks AS; Brouwer RW; Burns AJ; Cherny SS; Dopazo J; Eggen BJ; Griseri P; Jalloh B; Le TL; Lui VC; Luzón-Toro B; Matera I; Ngan ES; Pelet A; Ruiz-Ferrer M; Sham PC; Shepherd IT; So MT; Sribudiani Y; Tang CS; van den Hout MC; van der Linde HC; van Ham TJ; van IJcken WF; Verheij JB; Amiel J; Borrego S; Ceccherini I; Chakravarti A; Lyonnet S; Tam PK; Garcia-Barceló MM; Hofstra RM
    Genome Biol; 2017 Mar; 18(1):48. PubMed ID: 28274275
    [TBL] [Abstract][Full Text] [Related]  

  • 13. mirDNMR: a gene-centered database of background de novo mutation rates in human.
    Jiang Y; Li Z; Liu Z; Chen D; Wu W; Du Y; Ji L; Jin ZB; Li W; Wu J
    Nucleic Acids Res; 2017 Jan; 45(D1):D796-D803. PubMed ID: 27799474
    [TBL] [Abstract][Full Text] [Related]  

  • 14. De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability.
    McCarthy SE; Gillis J; Kramer M; Lihm J; Yoon S; Berstein Y; Mistry M; Pavlidis P; Solomon R; Ghiban E; Antoniou E; Kelleher E; O'Brien C; Donohoe G; Gill M; Morris DW; McCombie WR; Corvin A
    Mol Psychiatry; 2014 Jun; 19(6):652-8. PubMed ID: 24776741
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification of de novo germline mutations and causal genes for sporadic diseases using trio-based whole-exome/genome sequencing.
    Jin ZB; Li Z; Liu Z; Jiang Y; Cai XB; Wu J
    Biol Rev Camb Philos Soc; 2018 May; 93(2):1014-1031. PubMed ID: 29154454
    [TBL] [Abstract][Full Text] [Related]  

  • 16. mTADA is a framework for identifying risk genes from de novo mutations in multiple traits.
    Nguyen TH; Dobbyn A; Brown RC; Riley BP; Buxbaum JD; Pinto D; Purcell SM; Sullivan PF; He X; Stahl EA
    Nat Commun; 2020 Jun; 11(1):2929. PubMed ID: 32522981
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Whole Exome Sequencing Identifies Novel De Novo Variants Interacting with Six Gene Networks in Autism Spectrum Disorder.
    Kim N; Kim KH; Lim WJ; Kim J; Kim SA; Yoo HJ
    Genes (Basel); 2020 Dec; 12(1):. PubMed ID: 33374967
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Burden of de novo mutations and inherited rare single nucleotide variants in children with sensory processing dysfunction.
    Marco EJ; Aitken AB; Nair VP; da Gente G; Gerdes MR; Bologlu L; Thomas S; Sherr EH
    BMC Med Genomics; 2018 May; 11(1):50. PubMed ID: 29801487
    [TBL] [Abstract][Full Text] [Related]  

  • 19.
    Luo T; Li K; Ling Z; Zhao G; Li B; Wang Z; Wang X; Han Y; Xia L; Zhang Y; Zhou Q; Fang Z; Wang Y; Chen Q; Zhou X; Pan H; Zhao Y; Wang Y; Dong L; Huang Y; Hu Z; Pan Q; Xia K; Li J
    Comput Struct Biotechnol J; 2021; 19():1414-1422. PubMed ID: 33777337
    [TBL] [Abstract][Full Text] [Related]  

  • 20. EpiDenovo: a platform for linking regulatory de novo mutations to developmental epigenetics and diseases.
    Mao F; Liu Q; Zhao X; Yang H; Guo S; Xiao L; Li X; Teng H; Sun Z; Dou Y
    Nucleic Acids Res; 2018 Jan; 46(D1):D92-D99. PubMed ID: 29040751
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 34.